Filip Bošković

The paper shows that proteins in cell-like environments reduce RNA folding stability by passively suppressing base pairing, altering RNA structure predictions.

This study uses nanopore sensing to profile PEGylation of pegaptanib, revealing PEG heterogeneity and stability in serum.

The paper introduces RUNA, a reversible labeling chemistry to distinguish surface DNA from intracellular DNA on exosomes, revealing its role in immune cell interaction.

This paper introduces modular RNA:DNA nanostructures for direct, amplification-free rRNA profiling, enabling detection of rRNA variants and processing states.

This paper introduces a nanopore-based method to directly quantify RNA tandem repeats, achieving 18-nucleotide resolution and successfully detecting disease-associated repeats in DM1, DM2, and CCHS1.

This study compares two phosphate-activation chemistries' effects on nucleotide modifications, showing that primordial nucleotides are more susceptible to modification, which may explain the selection of the canonical genetic alphabet.

The paper compares the electrophoretic translocation dynamics of RNA:DNA hybrids and DNA:DNA duplexes through nanopores, finding that RNA:DNA hybrids translocate faster despite similar contour lengths.